| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| PCNX | Colorectal Cancer | p001_PCRC10 | Chr14:71455297:C>T | Branch mutation |
| PCNX | Colorectal Cancer | p004_CRC_A02 | Chr14:71568701:A>G | Private mutation |
| PCNX | Colorectal Cancer | p034_MSU2 | Chr14:71462521:T>A | Private mutation |
| PCNX | Colorectal Cancer | p034_MSU4 | Chr14:71575467:C>T | Private mutation |
| PCNX | Colorectal Cancer | p038_S | - | Branch mutation |
| PCNX | Colorectal Cancer | p040_case9 | Chr14:71374543:G>A | Trunk mutation |
| PCNX | Colorectal Cancer | p040_case9 | Chr14:71374546:A>G | Trunk mutation |
| PCNX | Colorectal Cancer | p147_a11 | p.V2209M | Trunk mutation |
| PCNX | Colorectal Cancer | p147_a20 | p.S880P | Trunk mutation |
| PCNX | Esophageal Squamous Cell Carcinoma | p124_ESCC024 | p.R2139W | Trunk mutation |
| PCNX | Esophageal Squamous Cell Carcinoma | p124_ESCC025 | p.V1226A | Private mutation |
| PCNX | Esophageal Squamous Cell Carcinoma | p128_P01 | Chr14:71374721:NA | Private mutation |
| PCNX | Esophageal Squamous Cell Carcinoma | p128_P21 | Chr14:71492926:G>A | Private mutation |
| PCNX | Esophageal Squamous Cell Carcinoma | p128_P24 | Chr14:71445269:C>T | Private mutation |
| PCNX | Esophageal Squamous Cell Carcinoma | p139_EC1111 | p.E418D | Private mutation |
| PCNX | Esophageal Squamous Cell Carcinoma | p139_EC1113 | p.L2013F | Branch mutation |
| PCNX | Gastric Adenocarcinoma | p011_MSS2 | p.R676Q | Private mutation |
| PCNX | Gastric Adenocarcinoma | p011_MSS3 | p.I1926V | Private mutation |
| PCNX | Gastric Adenocarcinoma | p011_MSI-H2 | p.L53F | Trunk mutation |
| PCNX | Gastric Carcinoma | p106_GC09 | p.S2157L | Private mutation |
| PCNX | Glioblastoma | p113_case03 | p.V841M | Trunk mutation |
| PCNX | Glioblastoma | p113_case07 | p.W1448* | Private mutation |
| PCNX | Glioblastoma | p113_case09 | p.E1005G | Private mutation |
| PCNX | Glioblastoma | p113_case18 | p.S928P | Private mutation |
| PCNX | Glioblastoma | p113_case26 | p.V549I | Private mutation |
| PCNX | Glioma | p168_P18 | p.S1507N | Private mutation |
| PCNX | Hepatocellular Carcinoma | p061_P03 | Chr14:71443671:A>G | Branch mutation |
| PCNX | Melanoma | p043_F | p.F1439Y | Trunk mutation |
| PCNX | Renal Cell Carcinoma | p073_RCC9 | Chr14:71570434:C>G | Private mutation |
| PCNX | Thyroid Cancer | p081_p2 | p.Q537N | Private mutation |
| PCNX | Urothelial Carcinoma | p031_WCM077 | p.R834C | Private mutation |